List of variants in gene NEXMIF reported as benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001008537.3(NEXMIF):c.2598C>A (p.Ser866=)	rs41298498	0.01502
NM_001008537.3(NEXMIF):c.2801A>G (p.Asn934Ser)	rs41306133	0.01057
NM_001008537.3(NEXMIF):c.151C>A (p.Pro51Thr)	rs145018752	0.00705
NM_001008537.3(NEXMIF):c.3798C>T (p.Gly1266=)	rs149185175	0.00527
NM_001008537.3(NEXMIF):c.2154T>C (p.Asn718=)	rs61741739	0.00368
NM_001008537.3(NEXMIF):c.3709A>T (p.Met1237Leu)	rs61731613	0.00368
NM_001008537.3(NEXMIF):c.2373A>C (p.Thr791=)	rs61742545	0.00315
NM_001008537.3(NEXMIF):c.4246C>T (p.Pro1416Ser)	rs143577015	0.00258
NM_001008537.3(NEXMIF):c.855A>G (p.Leu285=)	rs3762242	0.00184
NM_001008537.3(NEXMIF):c.4205A>G (p.Asn1402Ser)	rs140532942	0.00061
NM_001008537.3(NEXMIF):c.4509T>C (p.Pro1503=)	rs41303725	0.00055
NM_001008537.3(NEXMIF):c.2098G>C (p.Val700Leu)	rs141776597	0.00038
NM_001008537.3(NEXMIF):c.133G>A (p.Ala45Thr)	rs199960807	0.00030
NM_001008537.3(NEXMIF):c.42C>T (p.Asn14=)	rs370708043	0.00013
NM_001008537.3(NEXMIF):c.2672A>G (p.Asn891Ser)	rs186535459	0.00008

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.